FDA UDI In Commercial Distribution 🇺🇸 United States

Indy Standalone

DI: 00843210162140 · Model: SLV4530 · Altus Spine, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Indy Standalone
Primary DI
00843210162140
Version / Model
SLV4530
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-09
Public Version
2
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
3ded11e8-ab4e-4a5c-809e-f216430876dd

Device Description

Titanium Screw, 4.5mmx30mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 00843210162140

Customer Contacts

Phone
610-355-4156

Premarket Submissions

Submission Number Supplement Number
K211837 000